DentinogenesisImperfectaassociated with Type 1 OsteogenesisImperfecta: A Case Report
Journal Title: Saudi Journal of Medical and Pharmaceutical Sciences - Year 2018, Vol 4, Issue 7
Abstract
Abstract:DentinogenesisImperfecta is an autosomal dominant disorder of dentine affecting primary and permanent dentition. Mutation in dentinsialophospho protein on the long arm of chromosome 4 results in this defective dentin. The clinical appearance of teeth is characteristic showing an amber like translucency and severe attrition. It can also occur in association with osteogenesisImperfecta, a genetic disorder of type 1 collagen. Here we present a case of DentinogenesisImperfecta associated with Type 1 OsteogenesisImperfecta in a 14-year -old girl. Keywords: DentinogenesisImperfecta, OsteogenesisImperfecta.
Authors and Affiliations
Sreedevi P. U, Sreela L. S, Philips Mathew
Keywords
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